Trial Outcomes & Findings for Ultra-Brief Versus Brief Hands Only CPR Video Training With and Without Psychomotor Skill Practice (NCT NCT01191736)

Results Overview

Assessment of resuscitation skills using a Laerdal Resusci Annie recording manikin and Laerdal PC Skill Reporting software

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

336 participants

Primary outcome timeframe

60 minutes after intervention or two months after intervention

Results posted on

2011-03-07

Participant Flow

Participant milestones

Participant milestones
Measure	No Training, Assessed Within 60 Mins The subjects received no training and were assessed within 60 minutes	Ultra-brief Video; Assessed in 60 Mins Subjects receive an ultra-brief (90-second) video on hands-only CPR	Brief Video; Assessed in 60 Mins Subjects receive a brief (5-minute) video on hands-only CPR	Brief Video + hands-on; Ass'd in 60 Mins Subjects receive a brief (5-minute) video with hands-on manikin practice	Ultra-brief Video; Assessed at 2 Months Subjects receive an ultra-brief (90-second) video on hands-only CPR, and were assessed 2 months later	Brief Video; Assessed 2 Months Later Subjects receive a brief (5-minute) video on hands-only CPR, and were assessed two months later	Brief Video + hands-on; Ass'd 2 Months Later Subjects receive a brief (5-minute) video with hands-on manikin practice, and were assessed 2 months later
Overall Study STARTED	51	47	49	46	48	50	45
Overall Study COMPLETED	51	47	49	46	48	50	45
Overall Study NOT COMPLETED	0	0	0	0	0	0	0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Ultra-Brief Versus Brief Hands Only CPR Video Training With and Without Psychomotor Skill Practice

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure	No Training, Assessed Within 60 Mins n=51 Participants The subjects received no training and were assessed within 60 minutes	Ultra-brief Video; Assessed in 60 Mins n=47 Participants Subjects receive an ultra-brief (90-second) video on hands-only CPR	Brief Video; Assessed in 60 Mins n=49 Participants Subjects receive a brief (5-minute) video on hands-only CPR	Brief Video + hands-on; Ass'd in 60 Mins n=46 Participants Subjects receive a brief (5-minute) video with hands-on manikin practice	Ultra-brief Video; Assessed at 2 Months n=48 Participants Subjects receive an ultra-brief (90-second) video on hands-only CPR, and were assessed 2 months later	Brief Video; Assessed 2 Months Later n=50 Participants Subjects receive a brief (5-minute) video on hands-only CPR, and were assessed two months later	Brief Video + hands-on; Ass'd 2 Months Later n=45 Participants Subjects receive a brief (5-minute) video with hands-on manikin practice, and were assessed 2 months later	Total n=336 Participants Total of all reporting groups
Age, Categorical <=18 years	1 Participants n=5 Participants	1 Participants n=7 Participants	0 Participants n=5 Participants	3 Participants n=4 Participants	0 Participants n=21 Participants	2 Participants n=8 Participants	0 Participants n=8 Participants	7 Participants n=24 Participants
Age, Categorical Between 18 and 65 years	48 Participants n=5 Participants	32 Participants n=7 Participants	41 Participants n=5 Participants	39 Participants n=4 Participants	43 Participants n=21 Participants	44 Participants n=8 Participants	42 Participants n=8 Participants	289 Participants n=24 Participants
Age, Categorical >=65 years	2 Participants n=5 Participants	14 Participants n=7 Participants	8 Participants n=5 Participants	4 Participants n=4 Participants	5 Participants n=21 Participants	4 Participants n=8 Participants	3 Participants n=8 Participants	40 Participants n=24 Participants
Age Continuous	44.8 years STANDARD_DEVIATION 11.8 • n=5 Participants	51.7 years STANDARD_DEVIATION 15.2 • n=7 Participants	50.5 years STANDARD_DEVIATION 13.3 • n=5 Participants	41.7 years STANDARD_DEVIATION 14.2 • n=4 Participants	48.1 years STANDARD_DEVIATION 14.5 • n=21 Participants	45.3 years STANDARD_DEVIATION 13.8 • n=8 Participants	47.4 years STANDARD_DEVIATION 11.9 • n=8 Participants	47.1 years STANDARD_DEVIATION 13.8 • n=24 Participants
Sex: Female, Male Female	28 Participants n=5 Participants	28 Participants n=7 Participants	22 Participants n=5 Participants	29 Participants n=4 Participants	22 Participants n=21 Participants	27 Participants n=8 Participants	25 Participants n=8 Participants	181 Participants n=24 Participants
Sex: Female, Male Male	23 Participants n=5 Participants	19 Participants n=7 Participants	27 Participants n=5 Participants	17 Participants n=4 Participants	26 Participants n=21 Participants	23 Participants n=8 Participants	20 Participants n=8 Participants	155 Participants n=24 Participants
Region of Enrollment United States	51 participants n=5 Participants	47 participants n=7 Participants	49 participants n=5 Participants	46 participants n=4 Participants	48 participants n=21 Participants	50 participants n=8 Participants	45 participants n=8 Participants	336 participants n=24 Participants

PRIMARY outcome

Timeframe: 60 minutes after intervention or two months after intervention

Population: Per protocol

Assessment of resuscitation skills using a Laerdal Resusci Annie recording manikin and Laerdal PC Skill Reporting software

Outcome measures

Outcome measures
Measure	No Training, Assessed Within 60 Mins n=51 Participants The subjects received no training and were assessed within 60 minutes	Ultra-brief Video; Assessed in 60 Mins n=47 Participants Subjects receive an ultra-brief (90-second) video on hands-only CPR	Brief Video; Assessed in 60 Mins n=49 Participants Subjects receive a brief (5-minute) video on hands-only CPR	Brief Video + hands-on; Ass'd in 60 Mins n=46 Participants Subjects receive a brief (5-minute) video with hands-on manikin practice	Ultra-brief Video; Assessed at 2 Months n=48 Participants Subjects receive an ultra-brief (90-second) video on hands-only CPR, and were assessed 2 months later	Brief Video; Assessed 2 Months Later n=50 Participants Subjects receive a brief (5-minute) video on hands-only CPR, and were assessed two months later	Brief Video + hands-on; Ass'd 2 Months Later n=45 Participants Subjects receive a brief (5-minute) video with hands-on manikin practice, and were assessed 2 months later
Median Compression Depth (mm)	30 millimeters Interval 14.0 to 41.0	41 millimeters Interval 32.0 to 51.0	42 millimeters Interval 34.0 to 51.0	48 millimeters Interval 39.0 to 55.0	43 millimeters Interval 30.0 to 49.0	43 millimeters Interval 32.0 to 55.0	46 millimeters Interval 32.0 to 55.0

SECONDARY outcome

Timeframe: 60 minutes after intervention and two months after intervention

The proportion of the subjects who assessed the responsiveness of the victim (manikin) as judged by expert raters

Outcome measures

Outcome measures
Measure	No Training, Assessed Within 60 Mins n=51 Participants The subjects received no training and were assessed within 60 minutes	Ultra-brief Video; Assessed in 60 Mins n=47 Participants Subjects receive an ultra-brief (90-second) video on hands-only CPR	Brief Video; Assessed in 60 Mins n=49 Participants Subjects receive a brief (5-minute) video on hands-only CPR	Brief Video + hands-on; Ass'd in 60 Mins n=46 Participants Subjects receive a brief (5-minute) video with hands-on manikin practice	Ultra-brief Video; Assessed at 2 Months n=48 Participants Subjects receive an ultra-brief (90-second) video on hands-only CPR, and were assessed 2 months later	Brief Video; Assessed 2 Months Later n=50 Participants Subjects receive a brief (5-minute) video on hands-only CPR, and were assessed two months later	Brief Video + hands-on; Ass'd 2 Months Later n=45 Participants Subjects receive a brief (5-minute) video with hands-on manikin practice, and were assessed 2 months later
The Proportion of Subjects Who Assessed the Responsiveness of the Victim (Manikin) as Judged by Expert Raters	.854 Proportion of Participants Interval 0.754 to 0.954	.182 Proportion of Participants Interval 0.068 to 0.296	.8 Proportion of Participants Interval 0.683 to 0.917	.978 Proportion of Participants Interval 0.936 to 1.0	.542 Proportion of Participants Interval 0.401 to 0.683	.780 Proportion of Participants Interval 0.665 to 0.895	.822 Proportion of Participants Interval 0.711 to 0.934

Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

David Drachman

Maricopa Integrated Health System

Phone: 602-344-5161

Email: [email protected]

Results disclosure agreements

Principal investigator is a sponsor employee
Publication restrictions are in place